QC Scientist I
QC Scientist I
Posted on :
05-04-2025
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1 Vacancy
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Job Description
Work Schedule
Standard (MonFri)Environmental Conditions
Laboratory SettingJob Description
Summary:
In the role of QC Scientist I at Thermo Fisher Scientific perform analyses in a lab setting.
Essential Functions:
- Conduct moderately sophisticated chemical and physical testing of pharmaceutical raw materials packaging components finished products microbiological and stability samples using internally developed and validated test methods.
- Complete validated test methods for pharmaceutical raw materials and finished products resolving strength impurities identity and dissolution using HPLC GC LC/MS dissolution spectroscopy and traditional quantitative analysis.
- Recognize and report any outofspecification or unexpected results and nonroutine analytical and product issues recommending solutions.
- Maintain and troubleshoot analytical instrumentation as necessary.
- Clearly and accurately communicate results by detailing testing/analysis data and acquired results recording and reporting findings per prescribed lab procedures and systems. Collaborate with clients as needed.
- Prepare and assist in filing regulatory documents in support of internal projects. Communicate optimally with various departments corporate sites agencies and clients.
- Write SOPs and other instructional documents.
- Clean and coordinate the work area instrumentation and testing materials including HPLC and dissolution systems after use.
- Perform all duties in strict compliance with Standard Operating Procedures Good Manufacturing Practices Good Laboratory Practices and Safety guidelines maintaining vital compliance status per company and facility standards.
Education:
- Bachelors degree in a physical science preferably in Chemistry or Biology required.
Experience:
- 2 years of experience performing tests or analyses for pharmaceutical raw materials finished products or microbiological samples.
- Preferred experience with common office software and chromatographic data acquisition systems.
Equivalency:
- Equivalent combinations of education training and meaningful work experience may be considered.
Proficiencies:
- Solid understanding of chemistry and analytical instrumental technologies.
- Good knowledge of qualitative and quantitative chemical or microbiological analysis.
- Familiarity with quality and regulatory requirements in the pharmaceutical industry including GMPs and descriptive organic chemistry.
- Strong problemsolving skills and a logical approach to solving scientific problems.
- Proficiency with HPLC GC LC/MS and Dissolution techniques.
- Effective interpersonal and communication skills (oral and written).
- Competence in presenting information to customers clients and other employees.
- Ability to read analyze and interpret technical procedures and governmental regulations.
- Capability to write standard operating procedures protocols and reports.
- Ability to address common inquiries or complaints from customers or regulatory agencies.
- Proficiency in applying mathematical operations to determine test reliability analyze variance and apply correlation techniques.
Employment Type
Full-Time
Key Skills
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